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Title: Dissociation and reconstitution of a DNA polymerase alpha-primase complex. Author: Suzuki M, Enomoto T, Hanaoka F, Yamada M. Journal: J Biochem; 1985 Aug; 98(2):581-4. PubMed ID: 4066657. Abstract: The conditions for dissociation of the DNA polymerase alpha-primase complex (DNA polymerase alpha 1) have been examined. It was revealed that 50% ethylene glycol effectively dissociated the complex. The dissociated DNA polymerase and primase were purified to eliminate cross-contaminating activities by column chromatography using buffers containing 50% ethylene glycol. The sedimentation coefficients of the purified DNA polymerase and primase were 7.1S and 5.7S, respectively. These two enzymes were mixed in the presence of 20% ethylene glycol and the mixture was sedimented through a glycerol gradient containing no ethylene glycol. The DNA polymerase and primase activities co-sedimented at 9.1S which corresponds to the S value of intact alpha 1, indicating the reconstitution of the DNA polymerase alpha-primase complex.[Abstract] [Full Text] [Related] [New Search]